Microgenics Corp.
CEDIA DIGOXIN ASSAY (MODIFICATION)
SKU K920214UPC KXT
In Stock
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IIFDA 510(k) Cleared (K920214)
1
Free shipping on orders over $99 · 30-day returns
Microgenics Corp.
Free shipping on orders over $99 · 30-day returns
CEDIA DIGOXIN ASSAY (MODIFICATION) is an FDA 510(k)-cleared medical device (K920214) manufactured by Microgenics Corp.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 1, 1992. Regulation: 8.
